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Physiological and Proteomic Analysis of Penicillium digitatum in Response to X33 Antifungal Extract Treatment
Penicillium digitatum is a widespread pathogen among Rutaceae species that causes severe fruit decay symptoms on infected citrus fruit (known as citrus green mold). The employment of fungicides can effectively control the citrus green mold, significantly reducing agricultural economic loss. In this...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7677231/ https://www.ncbi.nlm.nih.gov/pubmed/33240238 http://dx.doi.org/10.3389/fmicb.2020.584331 |
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author | Lin, Shu-Hua Luo, Pan Yuan, En Zhu, Xiangdong Zhang, Bin Wu, Xiaoyu |
author_facet | Lin, Shu-Hua Luo, Pan Yuan, En Zhu, Xiangdong Zhang, Bin Wu, Xiaoyu |
author_sort | Lin, Shu-Hua |
collection | PubMed |
description | Penicillium digitatum is a widespread pathogen among Rutaceae species that causes severe fruit decay symptoms on infected citrus fruit (known as citrus green mold). The employment of fungicides can effectively control the citrus green mold, significantly reducing agricultural economic loss. In this study, we found that the X33 antifungal extract produced by Streptomyces lavendulae strain X33 inhibited the hyphae polarization of P. digitatum. Additionally, physiological and proteomic analysis strategies were applied to explore the inhibitory mechanism of the X33 antifungal extract of the S. lavendulae strain X33 on the mycelial growth of P. digitatum. A total of 277 differentially expressed proteins, consisting of 207 upregulated and 70 downregulated, were identified from the comparative proteomics analysis. The results indicated that the X33 antifungal extract induced mitochondrial membrane dysfunction and cellular integrity impairment, which can affect energy metabolism, oxidative stress, and transmembrane transport. The improved alkaline phosphatase activity and extracellular conductivity, increased H(2)O(2) and malondialdehyde contents, and inhibition of energy, amino acid, and sugar metabolism indicated that the oxidative stress of P. digitatum is induced by the X33 antifungal extract. These findings provided insight into the antifungal mechanism of the X33 antifungal extract against P. digitatum by suggesting that it may be an effective fungicide for controlling citrus postharvest green mold. |
format | Online Article Text |
id | pubmed-7677231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76772312020-11-24 Physiological and Proteomic Analysis of Penicillium digitatum in Response to X33 Antifungal Extract Treatment Lin, Shu-Hua Luo, Pan Yuan, En Zhu, Xiangdong Zhang, Bin Wu, Xiaoyu Front Microbiol Microbiology Penicillium digitatum is a widespread pathogen among Rutaceae species that causes severe fruit decay symptoms on infected citrus fruit (known as citrus green mold). The employment of fungicides can effectively control the citrus green mold, significantly reducing agricultural economic loss. In this study, we found that the X33 antifungal extract produced by Streptomyces lavendulae strain X33 inhibited the hyphae polarization of P. digitatum. Additionally, physiological and proteomic analysis strategies were applied to explore the inhibitory mechanism of the X33 antifungal extract of the S. lavendulae strain X33 on the mycelial growth of P. digitatum. A total of 277 differentially expressed proteins, consisting of 207 upregulated and 70 downregulated, were identified from the comparative proteomics analysis. The results indicated that the X33 antifungal extract induced mitochondrial membrane dysfunction and cellular integrity impairment, which can affect energy metabolism, oxidative stress, and transmembrane transport. The improved alkaline phosphatase activity and extracellular conductivity, increased H(2)O(2) and malondialdehyde contents, and inhibition of energy, amino acid, and sugar metabolism indicated that the oxidative stress of P. digitatum is induced by the X33 antifungal extract. These findings provided insight into the antifungal mechanism of the X33 antifungal extract against P. digitatum by suggesting that it may be an effective fungicide for controlling citrus postharvest green mold. Frontiers Media S.A. 2020-11-06 /pmc/articles/PMC7677231/ /pubmed/33240238 http://dx.doi.org/10.3389/fmicb.2020.584331 Text en Copyright © 2020 Lin, Luo, Yuan, Zhu, Zhang and Wu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Lin, Shu-Hua Luo, Pan Yuan, En Zhu, Xiangdong Zhang, Bin Wu, Xiaoyu Physiological and Proteomic Analysis of Penicillium digitatum in Response to X33 Antifungal Extract Treatment |
title | Physiological and Proteomic Analysis of Penicillium digitatum in Response to X33 Antifungal Extract Treatment |
title_full | Physiological and Proteomic Analysis of Penicillium digitatum in Response to X33 Antifungal Extract Treatment |
title_fullStr | Physiological and Proteomic Analysis of Penicillium digitatum in Response to X33 Antifungal Extract Treatment |
title_full_unstemmed | Physiological and Proteomic Analysis of Penicillium digitatum in Response to X33 Antifungal Extract Treatment |
title_short | Physiological and Proteomic Analysis of Penicillium digitatum in Response to X33 Antifungal Extract Treatment |
title_sort | physiological and proteomic analysis of penicillium digitatum in response to x33 antifungal extract treatment |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7677231/ https://www.ncbi.nlm.nih.gov/pubmed/33240238 http://dx.doi.org/10.3389/fmicb.2020.584331 |
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